A single genetic locus controls both expression of DPEP1/CHMP1A and kidney disease development via ferroptosis
Identifying causal variants and genes is an essential step in interpreting GWAS loci. Here, the authors investigate a kidney disease GWAS locus with functional genomics data, CRISPR editing and mouse experiments to identify DPEP1 and CHMP1A as putative kidney disease genes via ferroptosis.
Guardado en:
Autores principales: | Yuting Guan, Xiujie Liang, Ziyuan Ma, Hailong Hu, Hongbo Liu, Zhen Miao, Andreas Linkermann, Jacklyn N. Hellwege, Benjamin F. Voight, Katalin Susztak |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/94c00b491872474289c332bf354c853a |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
NUPR1 is a critical repressor of ferroptosis
por: Jiao Liu, et al.
Publicado: (2021) -
An autophagy assay reveals the ESCRT-III component CHMP2A as a regulator of phagophore closure
por: Yoshinori Takahashi, et al.
Publicado: (2018) -
GOT1 inhibition promotes pancreatic cancer cell death by ferroptosis
por: Daniel M. Kremer, et al.
Publicado: (2021) -
PTEN alleviates maladaptive repair of renal tubular epithelial cells by restoring CHMP2A-mediated phagosome closure
por: Huizhen Wang, et al.
Publicado: (2021) -
The balance between AIM2-associated inflammation and autophagy: the role of CHMP2A in brain injury after cardiac arrest
por: Rongjiao Shao, et al.
Publicado: (2021)